A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276959



Internal ID20486177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157522738..157522837hg38UCSC Ensembl
chr6:157943770..157943869hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737645
Supporting Variants
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276959
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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